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USG guided spinal Vs Blind spinal anaesthesia in obese patient

ULTRASONOGRAPHY GUIDED SUBARACHNOID BLOCK IN OBESE POPULATION - A COMPARISION OF TECHNICAL CHARACTERISTICS WITH LANDMARK GUIDED CONVENTIONAL BLIND APPROACH

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046144
Enrollment
100
Registered
2022-10-04
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Ultrasonography guided subarachnoid block in obese patients: Ultrasonography guided landmark noted and subarachnoid space located and timing and needle insertion and needle relocation t

Sponsors

Government of Gujarat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients eligible for surgery under subarachnoid block. Patient posted for elective surgery. Informed written consent BMI >30. Gender: Either ASA physical status I and II

Exclusion criteria

Exclusion criteria: Patient refusing consent Contraindication subarachnoid block, Infection at the site of injection. Bleeding and clotting disorders. Patient receiving medication affecting coagulation. Previous spine surgery or spine deformity. � Patients with neurological abnormality.

Design outcomes

Primary

MeasureTime frame
1)Time required to localise the mid-point of inter spinous space. 2)Time required for identification of subarachnoid space (Free flow of CSF through spinal needle). 3) Number of times needle redirected to obtained CSF (Number of passes). 4)The number of needle insertion attempts required to enter the subarachnoid space. 5)Traumatic needle puncture. (Blood coming out through needle). Timepoint: Continuous time monitoring on a stopwatch in seconds from start of procedure to the end of procedure.

Secondary

MeasureTime frame
1)Peri procedural subjective pain score. 2)Hemodynamic disturbance during procedure i.e. Tachycardia ,bradycardia,Hypertension,Hypotension,Arrythmia..Timepoint: All above parameters are observed at 1 min,5 min,10 min,15 min upto 30 min from start of procedure.

Countries

India

Contacts

Public ContactDrDCTripathi

B.J.medical college,civil hospital, Ahmedabad

drtripathi1961@yahoo.co.in9428408718

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026